홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

Ammonium formate → 6-(3-chloropropoxy)-7-methoxyquinazolin-4(3H)-one

HRID 1803019
노트
인쇄 미리보기

반응식

HRID 1803019 반응식
[NH2:1][C:2]1[CH:10]=[C:9]([O:11][CH3:12])[C:8]([O:13][CH2:14][CH2:15][CH2:16][Cl:17])=[CH:7][C:3]=1[C:4](O)=[O:5].[CH:18]([O-])=O.[NH4+:21]>C(N)=O>[Cl:17][CH2:16][CH2:15][CH2:14][O:13][C:8]1[CH:7]=[C:3]2[C:2](=[CH:10][C:9]=1[O:11][CH3:12])[N:1]=[CH:18][NH:21][C:4]2=[O:5]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 2723923Ammonium formateHCID 230329942-Amino-4-methoxy-5-(3-chloropropoxy)benzoic acid

생성물 1

HCID 1355897736-(3-chloropropoxy)-7-methoxyquinazolin-4(3H)-one수율 90.2%

시약·촉매·용매 1

HCID 713Formamide용매

반응 조건

온도
47.5 °C

실험 절차

2-amino-4-methoxy-5-(3-chloropropoxy)benzoic acid (450 gm), formamide (2250 ml) and ammonium formate (200 gm) were heated to 170-180° C. for 3-4 hours. The reaction mass was concentrated under reduced pressure at 140-150° C. The residue was stirred in methanol (1000 ml) at 45-50° C. and cooled to 5-10° C. The solid obtained was filtered to yield the title compound (420 gm, 90% yield).

후처리

  1. concentrationThe reaction mass was concentrated under reduced pressure at 140-150° C
  2. temperaturecooled to 5-10° C
  3. customThe solid obtained
  4. filtrationwas filtered

출처 및 근거

ORD 기록
ord-6265f294127543ef9d1b5928c01b3d66
출처 데이터셋
uspto-grants-2013_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08350029B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트